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3-hydroxybutyric acid and Pancreatitis

3-hydroxybutyric acid has been researched along with Pancreatitis in 7 studies

3-Hydroxybutyric Acid: BUTYRIC ACID substituted in the beta or 3 position. It is one of the ketone bodies produced in the liver.
3-hydroxybutyric acid : A straight-chain 3-hydroxy monocarboxylic acid comprising a butyric acid core with a single hydroxy substituent in the 3- position; a ketone body whose levels are raised during ketosis, used as an energy source by the brain during fasting in humans. Also used to synthesise biodegradable plastics.

Pancreatitis: INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis.

Research Excerpts

ExcerptRelevanceReference
"To evaluate the effects of acute pancreatitis on the energy metabolism of the liver and on the fragility of hepatic cells and subcellular organelles, we studies (1) the arterial blood ketone body ratio (BKBR) (aceto acetate/beta-hydroxy butyrate), which is in equilibrium with the free NAD+/NADH ratio in liver mitochondria; (2) the hepatic energy charge (EC) = (ATP + 1/2 ADP)/(ATP + ADP + AMP); (3) the cathepsin B leakage from hepatic lysosomes and the malate dehydrogenase leakage from hepatic mitochondria in vitro; and (4) the protective effects of prostaglandin E2 (PGE2) and a new synthetic protease inhibitor ONO 3307 on hepatic injury in acute pancreatitis induced in rats by a supramaximal dose of caerulein."7.68Impaired hepatic energy metabolism in rat acute pancreatitis: protective effects of prostaglandin E2 and synthetic protease inhibitor ONO 3307. ( Hirano, T; Manabe, T; Tobe, T, 1992)
"To evaluate the effects of acute pancreatitis on the energy metabolism of the liver and on the fragility of hepatic cells and subcellular organelles, we studies (1) the arterial blood ketone body ratio (BKBR) (aceto acetate/beta-hydroxy butyrate), which is in equilibrium with the free NAD+/NADH ratio in liver mitochondria; (2) the hepatic energy charge (EC) = (ATP + 1/2 ADP)/(ATP + ADP + AMP); (3) the cathepsin B leakage from hepatic lysosomes and the malate dehydrogenase leakage from hepatic mitochondria in vitro; and (4) the protective effects of prostaglandin E2 (PGE2) and a new synthetic protease inhibitor ONO 3307 on hepatic injury in acute pancreatitis induced in rats by a supramaximal dose of caerulein."3.68Impaired hepatic energy metabolism in rat acute pancreatitis: protective effects of prostaglandin E2 and synthetic protease inhibitor ONO 3307. ( Hirano, T; Manabe, T; Tobe, T, 1992)
"Acute pancreatitis and hyperamylasemia are often seen in patients with acute liver failure (ALF)."1.72β-hydroxybutyrate inhibits ferroptosis-mediated pancreatic damage in acute liver failure through the increase of H3K9bhb. ( Chen, J; Cui, B; Li, B; Li, X; Liu, J; Liu, L; Shan, C; Sun, N; Sun, W; Xing, H; Xu, Q; Yang, T; Zheng, Y; Zhu, W, 2022)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's2 (28.57)18.2507
2000's0 (0.00)29.6817
2010's1 (14.29)24.3611
2020's3 (42.86)2.80

Authors

AuthorsStudies
Şahin, E1
Bektur Aykanat, NE1
Kacar, S1
Bagci, R1
Sahinturk, V1
Zhang, L1
Shi, J1
Du, D1
Niu, N1
Liu, S1
Yang, X1
Lu, P1
Shen, X1
Shi, N1
Yao, L1
Zhang, R1
Hu, G1
Lu, G1
Zhu, Q1
Zeng, T1
Liu, T1
Xia, Q1
Huang, W1
Xue, J1
Zheng, Y1
Sun, W1
Shan, C1
Li, B1
Liu, J1
Xing, H1
Xu, Q1
Cui, B1
Zhu, W1
Chen, J1
Liu, L1
Yang, T1
Sun, N1
Li, X1
Hurrell, FE1
Drobatz, KJ1
Hess, RS1
Hirano, T1
Manabe, T1
Tobe, T1
Larsen, S1
Hilsted, J1
Philipsen, EK1
Tronier, B1
Damkjaer Nielsen, M1
Worning, H1
Fulop, M1
Bock, J1
Ben-Ezra, J1
Antony, M1
Danzig, J1
Gage, JS1

Other Studies

7 other studies available for 3-hydroxybutyric acid and Pancreatitis

ArticleYear
β-Hydroxybutyrate, One of the Three Main Ketone Bodies, Ameliorates Acute Pancreatitis in Rats by Suppressing the NLRP3 Inflammasome Pathway.
    The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2021, Volume: 32, Issue:8

    Topics: 3-Hydroxybutyric Acid; Animals; Inflammasomes; Male; NLR Family, Pyrin Domain-Containing 3 Protein;

2021
Ketogenesis acts as an endogenous protective programme to restrain inflammatory macrophage activation during acute pancreatitis.
    EBioMedicine, 2022, Volume: 78

    Topics: 3-Hydroxybutyric Acid; Acute Disease; Adolescent; Animals; Ceruletide; China; Disease Models, Animal

2022
β-hydroxybutyrate inhibits ferroptosis-mediated pancreatic damage in acute liver failure through the increase of H3K9bhb.
    Cell reports, 2022, 12-20, Volume: 41, Issue:12

    Topics: 3-Hydroxybutyric Acid; Acute Disease; Animals; Ferroptosis; Hyperamylasemia; Liver Failure, Acute; M

2022
Beta-hydroxybutyrate Concentrations in Dogs with Acute Pancreatitis and Without Diabetes Mellitus.
    Journal of veterinary internal medicine, 2016, Volume: 30, Issue:3

    Topics: 3-Hydroxybutyric Acid; Acute Disease; Animals; Anorexia; Dog Diseases; Dogs; Fasting; Pancreatitis;

2016
Impaired hepatic energy metabolism in rat acute pancreatitis: protective effects of prostaglandin E2 and synthetic protease inhibitor ONO 3307.
    The Journal of surgical research, 1992, Volume: 53, Issue:3

    Topics: 3-Hydroxybutyric Acid; Acetoacetates; Acute Disease; Adenosine Diphosphate; Adenosine Triphosphate;

1992
The effect of insulin withdrawal on intermediary metabolism in patients with diabetes secondary to chronic pancreatitis.
    Acta endocrinologica, 1991, Volume: 124, Issue:5

    Topics: 3-Hydroxybutyric Acid; Adult; Blood Glucose; Chronic Disease; Diabetes Mellitus, Type 1; Epinephrine

1991
Plasma lactate and 3-hydroxybutyrate levels in patients with acute ethanol intoxication.
    The American journal of medicine, 1986, Volume: 80, Issue:2

    Topics: 3-Hydroxybutyric Acid; Acute Disease; Adult; Aged; Alcoholic Intoxication; Blood Glucose; Diabetic K

1986